Internal Paddles Option For Defibrillator/monitor (2020-09-17)

Recall Summary Internal paddles for certain defibrillator/monitor devices are being recalled across Canada due to a medical device issue. The recall is classified as Class I, indicating a serious safety concern. This affects users of the affected defibrillator/monitor models that have internal paddle options.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2020-10-09

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/c769d3a5-cee2-4e66-9802-36697ff1cd25